Джерело:
Ця вакансія не має повного перекладу вибраною мовою. Нижче показано оригінальний зміст.
Дата публікації: 01.11.2026
Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We focus on the most complex trials, the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize biotech companies to move promising therapies through early phase development, so they reach the patients sooner.
Responsibilities
Collects, validates, and maintains data from internal and external sources to support feasibility and operational activities; Analyses clinical trial, site, investigator, and operational data to identify trends, patterns, and opportunities for improvement; Develops and maintains standard reports, dashboards, and data visualizations to support stakeholder decision-making; Supports feasibility assessments by providing data summaries, analyses, and insights related to study requirements, site performance, recruitment trends, and therapeutic areas; Collaborates with Operational Strategy, Clinical Operations, Business Development, and other functional stakeholders to understand data needs and deliver timely analyses; Performs data quality reviews and works to resolve data inconsistencies and gaps; Identifies opportunities to improve existing data collection, reporting, and analytical processes; Supports the evaluation and integration of new data sources, tools, and technologies; Maintains documentation related to data sources, methodologies, reporting processes, and best practices; Develops and updates reporting templates and analytical tools to improve efficiency and consistency; Provides ad hoc analyses and reports in support of departmental and organizational priorities; Monitors key operational and feasibility metrics and communicates findings to stakeholders; Supports process improvement initiatives by leveraging data to identify efficiencies and operational enhancements; Ensures compliance with applicable quality standards, policies, and data governance requirements; Performs other duties and special projects as assignedRequirements
Bachelor's degree in Life Sciences, Data Analytics, Health Sciences, Business, Statistics, Public Health, or a related field; Strong experience in clinical research, feasibility, clinical operations, data analytics, business intelligence, or a related field; Experience working with clinical trial, investigator, site, operational, or healthcare-related datasets; Demonstrated experience analysing and interpreting complex data from multiple sources; Experience developing reports, dashboards, and data visualizations for business stakeholders; Experience collaborating with cross-functional teams in a global environmentNice to have
Master's degree in a relevant discipline; Experience working within a CRO, pharmaceutical, biotechnology, healthcare, or related environment; Experience supporting feasibility assessments, site selection activities, clinical operations, or operational planning; Knowledge of clinical development processes and clinical trial conduct; Experience with business intelligence and reporting tools such as Power BI, Tableau, Spotfire, or similar platformsЯк відгукнутися
Подати заявку онлайн: https://www.jobs.pl/uk/oferta/100894612/aplikuj
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